Abstract
The distribution and dissociation equilibria of phase-transfer catalyst, trioctylmethyl-ammonium chloride (Q +Cl− ), for the system of QCl–toluene–aqueous HCrO4 − solutions were measured at 298K for the systems of toluene–water or –aqueous electrolyte solutions.
The evaluated distribution coefficients of trioctylmethylammonium chloride and the complex formed between trioctylmethylammonium cation and HCrO4 − were correlated as a function of the ionic strength in the aqueous solutions. The dissociation constants, K 1 and K 2, were independent of ionic strength.
Acknowledgments
This work was supported by Grant No. 2000-2-30700-002-3 from the Basic Research Program of the Korea Science & Engineering Foundation.